* The position: Your task consists of two major parts: to coordinate the device documentation work, on the one hand and to conduct the safety risk analyses for the devices used in clinical drug trials, on the other hand. Being the representative of the devices used, you will coordinate among several independently working drug trials. This is not limited to organising and conducting meetings and workshops with members of various areas in Novo Nordisk, demonstrating device use for project members and preparing risk summary documentation for regulatory purposes. You will be given a broad range of responsibilities and experience a variety of tasks, working with stakeholders at all levels. The job will enhance your professional and personal development, providing you with an opportunity to further develop your skills within specialist expertise and project management.